Higher target capture efficiency using probe extension

ABSTRACT

Aspects of the invention include methods for preparing an enriched sequencing library. In some embodiments, the methods involve preparing a sequencing library that is enriched for AT-rich sequences. In certain embodiments, the methods involve determining a presence or an absence of cancer, determining a cancer stage, monitoring cancer progression, and/or determining a cancer classification in a subject by analyzing an enriched sequencing library.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority benefit of the filing date of U.S. Provisional Patent Application Ser. No. 62/480,199, filed on Mar. 31, 2017, the disclosure of which application is herein incorporated by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to molecular biology techniques and methods for preparing targeted sequencing libraries.

BACKGROUND OF THE INVENTION

Analysis of circulating cell-free nucleic acids (e.g., cfDNA or cfRNA) using next generation sequencing (NGS) is recognized as a valuable tool for detection and diagnosis of cancer. Current protocols for preparing cell-free nucleic acids for sequencing typically include targeted enrichment to isolate targeted nucleic acid sequences from a library for further analysis. However, AT-rich sequences can be lost during library preparation and subsequent washing steps due to low probe-target hybridization (e.g., due to low melting temperature of high AT rich regions). Non-target, or off-target nucleic acids can also be carried over after enrichment due to nonspecific bindings and adapter-to-adapter bindings due to insufficient washing, which can result in a significant reduction of on-target nucleic acid sequences. Accordingly, there remains a need in the art for more efficient methods for preparing targeted sequencing libraries.

SUMMARY OF THE INVENTION

Aspects of the invention include methods for preparing an enriched sequencing library. In some embodiments, a method for preparing an enriched sequencing library involves (a) obtaining a test sample comprising a plurality of cell-free nucleic acid (cfNA) fragments; (b) preparing a sequencing library from the cfNA fragments; (c) enriching the sequencing library by: i. adding a plurality of capture probes to the sequencing library, wherein the plurality of capture probes are designed to be complementary to one or more regions of one or more target nucleic acids; ii. hybridizing the plurality of capture probes to the one or more target nucleic acids; iii. extending the capture probes using a polymerase and the target nucleic acids as a template to generate a plurality of extended probe-target nucleic acid constructs; and iv. isolating the plurality of extended probe-target nucleic acid constructs to generate the enriched sequencing library.

In some embodiments, a method for preparing a sequencing library enriched for AT-rich sequences involves (a) obtaining a test sample comprising a plurality of cell-free nucleic acid fragments; (b) preparing a sequencing library from the plurality of cfNA fragments; (c) enriching the sequencing library for AT-rich nucleic acid fragments by: i. adding a plurality of capture probes to the sequencing library, wherein the plurality of capture probes are designed to be complementary to one or more regions of one or more target nucleic acids; ii. hybridizing the plurality of capture probes to the one or more target nucleic acids; iii. extending the capture probes using a polymerase and the target nucleic acids as templates to generate a plurality of extended probe-target nucleic acid constructs; and iv. isolating the plurality of extended probe-target nucleic acid constructs to generate the enriched sequencing library; wherein the sequencing library is enriched for AT rich sequences compared to a non-enriched sequencing library.

In some embodiments, a method for detecting a presence or absence of cancer, determining cancer stage, monitoring cancer progression, and/or determining a cancer classification in a subject involves: (a) obtaining a test sample comprising a plurality of cell-free nucleic acid (cfNA) fragments, wherein the test sample is from a subject known to have, or suspected of having, cancer; (b) preparing a sequencing library from the cfNA fragments; (c) enriching the sequencing library for one or more target nucleic acids, wherein enriching the sequencing library comprises: i. adding a plurality of capture probes to the sequencing library, wherein the plurality of capture probes are complementary to one or more target regions of one or more target nucleic acids; ii. hybridizing the plurality of capture probes to the one or more target nucleic acids; iii. extending the capture probes using a polymerase and the one or more target nucleic acids as a template to generate a plurality of extended probe-target nucleic acid constructs; and iv. isolating the plurality of extended probe-target nucleic acid constructs to generate the enriched sequencing library; (d) sequencing the enriched sequencing library to obtain a plurality of sequence reads; and (e) analyzing the one or more target nucleic acids in the plurality of sequence reads to detect the presence or absence of cancer, determine cancer status, monitor cancer progression and/or determine a cancer classification.

In some embodiments, the cell-free nucleic acids (cfNAs) are cell-free DNA (cfDNA) fragments. In some embodiments, the cell-free nucleic acids (cfNAs) are cell-free RNA (cfRNA) fragments. In some embodiments, the cell-free nucleic acids (cfNAs) are cell-free DNA (cfDNA) fragments and cell-free RNA (cfRNA) fragments.

In some embodiments, the plurality of capture probes range in length from about 20 nt to about 200 nt. In some embodiments, the plurality of capture probes are each less than about 60 nt in length. In some embodiments, the plurality of capture probes are each less than about 40 nt in length.

In some embodiments, the plurality of capture probes comprise a set of probes designed to hybridize with nucleic acid fragments from about 5 to about 10,000 target regions. In some embodiments, the plurality of capture probes comprises a set of capture probes designed to hybridize with sense strands and antisense strands of a plurality of target nucleic acids.

In some embodiments, a method improves an isolation efficiency for sense strands and their complementary antisense strands. In some embodiments, the polymerase is a DNA polymerase having strand-displacement activity. In some embodiments, the plurality of capture probes are biotinylated. In some embodiments, the plurality of extended probe-target nucleic acids are isolated using streptavidin-coated beads.

In some embodiments, the cell-free nucleic acid test sample comprises whole blood, a blood fraction, plasma, serum, urine, fecal, saliva, a tissue biopsy, pleural fluid, pericardial fluid, cerebral spinal fluid, peritoneal fluid, or any combination thereof. In some embodiments, the cell-free nucleic acid is a plasma sample obtained from a patient known to have, or suspected of having cancer. In some embodiments, the cell-free nucleic acid test sample comprises nucleic acids originating from healthy cells and from cancer cells.

In some embodiments, the plurality of capture probes comprises a probe set comprising one or more capture probes for one or more single nucleotide variants (SNVs), indels, fusion events and/or copy number alterations (CNAs).

In some embodiments, the sequence reads are obtained from a next-generation sequencing (NGS) procedure. In some embodiments, sequencing the enriched sequencing library lowers a sequencing depth requirement for detecting the presence or absence of cancer, determining cancer status, monitoring cancer progression and/or determining a cancer classification, compared to a sequencing depth requirement for a non-enriched sequencing library. In some embodiments, the sequence reads are obtained from massively parallel sequencing using a sequencing-by-synthesis procedure. In some embodiments, the sequence reads are obtained from a paired-end sequencing procedure. In some embodiments, the sequence reads are identified based on alignment of the sequence reads to a reference genome, or to a portion of a reference genome. In some embodiments, the sequence reads are identified based on a de novo assembly procedure.

In some embodiments, monitoring cancer progression further comprises monitoring disease progression, monitoring therapy, or monitoring cancer growth. In some embodiments, the cancer classification comprises determining a cancer type and/or a cancer tissue of origin.

In some embodiments, the cancer comprises a carcinoma, a sarcoma, a myeloma, a leukemia, a lymphoma, a blastoma, a germ cell tumor, or any combination thereof. In some embodiments, the carcinoma is an adenocarcinoma. In some embodiments, the carcinoma is a squamous cell carcinoma. In some embodiments, the carcinoma is selected from the group consisting of: small cell lung, non-small-cell lung, nasopharyngeal, colorectal, anal, liver, urinary bladder, cervical, testicular, ovarian, gastric, esophageal, head-and-neck, pancreatic, prostate, renal, thyroid, melanoma, and breast carcinoma. In some embodiments, the sarcoma is selected from the group consisting of: osteosarcoma, chondrosarcoma, leiomyosarcoma, rhabdomyosarcoma, mesothelial sarcoma (mesothelioma), fibrosarcoma, angiosarcoma, liposarcoma, glioma, and astrocytoma. In some embodiments, the leukemia is selected from the group consisting of: myelogenous, granulocytic, lymphatic, lymphocytic, and lymphoblastic leukemia. In some embodiments, the lymphoma is selected from the group consisting of: Hodgkin's lymphoma and Non-Hodgkin's lymphoma.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a flow diagram illustrating a method for preparing a sequencing library prepared in accordance with one embodiment of the present invention.

FIG. 2 is an illustration showing pictorially the steps of the method described in FIG. 1.

FIG. 3 is a flow diagram illustrating a method for analyzing sequence reads for cancer detection, status and/or classification utilizing a sequencing library prepared in accordance with one embodiment of the present invention.

FIGS. 4A and 4B are bar graphs illustrating mean, and raw base coverage, respectively, using extended (PEX) and non-extended capture probes to isolate targeted DNA fragments.

FIG. 5 is a bar graph illustrating drop out for AT-rich DNA fragments (AT) and GC-rich (GC) DNA fragments.

FIG. 6 is a bar graph illustrating normalized coverage for raw and collapsed sequence reads from PEX and SOP samples.

FIG. 7 is a dot plot illustrating the ratio of raw normalized coverage for each enriched target region plotted against the % GC content of the targets.

FIGS. 8A and 8B are plots for two separate sequencing runs, respectively, illustrating collapsed coverage across targeted nucleic acids (for targets 1, 10, 20, 30, 40 and 50).

DEFINITIONS

Before the present invention is described in greater detail, it is to be understood that this invention is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.

Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit, unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges encompassed within the invention, subject to any specifically excluded limit in the stated range.

Unless defined otherwise, technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Singleton et al., Dictionary of Microbiology and Molecular Biology 2nd ed., J. Wiley & Sons (New York, N.Y. 1994), provides one skilled in the art with a general guide to many of the terms used in the present application, as do the following, each of which is incorporated by reference herein in its entirety: Kornberg and Baker, DNA Replication, Second Edition (W.H. Freeman, New York, 1992); Lehninger, Biochemistry, Second Edition (Worth Publishers, New York, 1975); Strachan and Read, Human Molecular Genetics, Second Edition (Wiley-Liss, New York, 1999); Abbas et al, Cellular and Molecular Immunology, 6^(th) edition (Saunders, 2007).

All publications mentioned herein are expressly incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited.

The term “amplicon” as used herein means the product of a polynucleotide amplification reaction; that is, a clonal population of polynucleotides, which may be single stranded or double stranded, which are replicated from one or more starting sequences. The one or more starting sequences may be one or more copies of the same sequence, or they may be a mixture of different sequences. Preferably, amplicons are formed by the amplification of a single starting sequence. Amplicons may be produced by a variety of amplification reactions whose products comprise replicates of the one or more starting, or target, nucleic acids. In one aspect, amplification reactions producing amplicons are “template-driven” in that base pairing of reactants, either nucleotides or oligonucleotides, have complements in a template polynucleotide that are required for the creation of reaction products. In one aspect, template-driven reactions are primer extensions with a nucleic acid polymerase, or oligonucleotide ligations with a nucleic acid ligase. Such reactions include, but are not limited to, polymerase chain reactions (PCRs), linear polymerase reactions, nucleic acid sequence-based amplification (NASBAs), rolling circle amplifications, and the like, disclosed in the following references, each of which are incorporated herein by reference herein in their entirety: Mullis et al, U.S. Pat. Nos. 4,683,195; 4,965,188; 4,683,202; 4,800,159 (PCR); Gelfand et al, U.S. Pat. No. 5,210,015 (real-time PCR with “taqman” probes); Wittwer et al, U.S. Pat. No. 6,174,670; Kacian et al, U.S. Pat. No. 5,399,491 (“NASBA”); Lizardi, U.S. Pat. No. 5,854,033; Aono et al, Japanese patent publ. JP 4-262799 (rolling circle amplification); and the like. In one aspect, amplicons of the invention are produced by PCRs. An amplification reaction may be a “real-time” amplification if a detection chemistry is available that permits a reaction product to be measured as the amplification reaction progresses, e.g., “real-time PCR”, or “real-time NASBA” as described in Leone et al, Nucleic Acids Research, 26: 2150-2155 (1998), and like references.

As used herein, the term “amplifying” means performing an amplification reaction. A “reaction mixture” means a solution containing all the necessary reactants for performing a reaction, which may include, but is not be limited to, buffering agents to maintain pH at a selected level during a reaction, salts, co-factors, scavengers, and the like.

The terms “fragment” or “segment”, as used interchangeably herein, refer to a portion of a larger polynucleotide molecule. A polynucleotide, for example, can be broken up, or fragmented into, a plurality of segments, either through natural processes, as is the case with, e.g., cfDNA fragments that can naturally occur within a biological sample, or through in vitro manipulation. Various methods of fragmenting nucleic acids are well known in the art. These methods may be, for example, either chemical or physical or enzymatic in nature. Enzymatic fragmentation may include partial degradation with a DNase; partial depurination with acid; the use of restriction enzymes; intron-encoded endonucleases; DNA-based cleavage methods, such as triplex and hybrid formation methods, that rely on the specific hybridization of a nucleic acid segment to localize a cleavage agent to a specific location in the nucleic acid molecule; or other enzymes or compounds which cleave a polynucleotide at known or unknown locations. Physical fragmentation methods may involve subjecting a polynucleotide to a high shear rate. High shear rates may be produced, for example, by moving DNA through a chamber or channel with pits or spikes, or forcing a DNA sample through a restricted size flow passage, e.g., an aperture having a cross sectional dimension in the micron or submicron range. Other physical methods include sonication and nebulization. Combinations of physical and chemical fragmentation methods may likewise be employed, such as fragmentation by heat and ion-mediated hydrolysis. See, e.g., Sambrook et al., “Molecular Cloning: A Laboratory Manual,” 3rd Ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001) (“Sambrook et al.) which is incorporated herein by reference for all purposes. These methods can be optimized to digest a nucleic acid into fragments of a selected size range.

The terms “polymerase chain reaction” or “PCR”, as used interchangeably herein, mean a reaction for the in vitro amplification of specific DNA sequences by the simultaneous primer extension of complementary strands of DNA. In other words, PCR is a reaction for making multiple copies or replicates of a target nucleic acid flanked by primer binding sites, such reaction comprising one or more repetitions of the following steps: (i) denaturing the target nucleic acid, (ii) annealing primers to the primer binding sites, and (iii) extending the primers by a nucleic acid polymerase in the presence of nucleoside triphosphates. Usually, the reaction is cycled through different temperatures optimized for each step in a thermal cycler instrument. Particular temperatures, durations at each step, and rates of change between steps depend on many factors that are well-known to those of ordinary skill in the art, e.g., exemplified by the following references: McPherson et al, editors, PCR: A Practical Approach and PCR2: A Practical Approach (IRL Press, Oxford, 1991 and 1995, respectively). For example, in a conventional PCR using Taq DNA polymerase, a double stranded target nucleic acid may be denatured at a temperature>90° C., primers annealed at a temperature in the range 50-75° C., and primers extended at a temperature in the range 72-78° C. The term “PCR” encompasses derivative forms of the reaction, including, but not limited to, RT-PCR, real-time PCR, nested PCR, quantitative PCR, multiplexed PCR, and the like. The particular format of PCR being employed is discernible by one skilled in the art from the context of an application. Reaction volumes can range from a few hundred nanoliters, e.g., 200 nL, to a few hundred μL, e.g., 200 μL. “Reverse transcription PCR,” or “RT-PCR,” means a PCR that is preceded by a reverse transcription reaction that converts a target RNA to a complementary single stranded DNA, which is then amplified, an example of which is described in Tecott et al, U.S. Pat. No. 5,168,038, the disclosure of which is incorporated herein by reference in its entirety. “Real-time PCR” means a PCR for which the amount of reaction product, i.e., amplicon, is monitored as the reaction proceeds. There are many forms of real-time PCR that differ mainly in the detection chemistries used for monitoring the reaction product, e.g., Gelfand et al, U.S. Pat. No. 5,210,015 (“taqman”); Wittwer et al, U.S. Pat. Nos. 6,174,670 and 6,569,627 (intercalating dyes); Tyagi et al, U.S. Pat. No. 5,925,517 (molecular beacons); the disclosures of which are hereby incorporated by reference herein in their entireties. Detection chemistries for real-time PCR are reviewed in Mackay et al, Nucleic Acids Research, 30: 1292-1305 (2002), which is also incorporated herein by reference. “Nested PCR” means a two-stage PCR wherein the amplicon of a first PCR becomes the sample for a second PCR using a new set of primers, at least one of which binds to an interior location of the first amplicon. As used herein, “initial primers” in reference to a nested amplification reaction mean the primers used to generate a first amplicon, and “secondary primers” mean the one or more primers used to generate a second, or nested, amplicon. “Asymmetric PCR” means a PCR wherein one of the two primers employed is in great excess concentration so that the reaction is primarily a linear amplification in which one of the two strands of a target nucleic acid is preferentially copied. The excess concentration of asymmetric PCR primers may be expressed as a concentration ratio. Typical ratios are in the range of from 10 to 100. “Multiplexed PCR” means a PCR wherein multiple target sequences (or a single target sequence and one or more reference sequences) are simultaneously carried out in the same reaction mixture, e.g., Bernard et al, Anal. Biochem., 273: 221-228 (1999)(two-color real-time PCR). Usually, distinct sets of primers are employed for each sequence being amplified. Typically, the number of target sequences in a multiplex PCR is in the range of from 2 to 50, or from 2 to 40, or from 2 to 30. “Quantitative PCR” means a PCR designed to measure the abundance of one or more specific target sequences in a sample or specimen. Quantitative PCR includes both absolute quantitation and relative quantitation of such target sequences. Quantitative measurements are made using one or more reference sequences or internal standards that may be assayed separately or together with a target sequence. The reference sequence may be endogenous or exogenous to a sample or specimen, and in the latter case, may comprise one or more competitor templates. Typical endogenous reference sequences include segments of transcripts of the following genes: β-actin, GAPDH, β₂-microglobulin, ribosomal RNA, and the like. Techniques for quantitative PCR are well-known to those of ordinary skill in the art, as exemplified in the following references, which are incorporated by reference herein in their entireties: Freeman et al, Biotechniques, 26: 112-126 (1999); Becker-Andre et al, Nucleic Acids Research, 17: 9437-9447 (1989); Zimmerman et al, Biotechniques, 21: 268-279 (1996); Diviacco et al, Gene, 122: 3013-3020 (1992); and Becker-Andre et al, Nucleic Acids Research, 17: 9437-9446 (1989).

The term “primer” as used herein means an oligonucleotide, either natural or synthetic, that is capable, upon forming a duplex with a polynucleotide template, of acting as a point of initiation of nucleic acid synthesis and being extended from its 3′-end along the template so that an extended duplex is formed. Extension of a primer is usually carried out with a nucleic acid polymerase, such as a DNA or RNA polymerase. The sequence of nucleotides added in the extension process is determined by the sequence of the template polynucleotide. Usually, primers are extended by a DNA polymerase. Primers usually have a length in the range of from 14 to 40 nucleotides, or in the range of from 18 to 36 nucleotides. Primers are employed in a variety of nucleic acid amplification reactions, for example, linear amplification reactions using a single primer, or polymerase chain reactions, employing two or more primers. Guidance for selecting the lengths and sequences of primers for particular applications is well known to those of ordinary skill in the art, as evidenced by the following reference that is incorporated by reference herein in its entirety: Dieffenbach, editor, PCR Primer: A Laboratory Manual, 2^(nd) Edition (Cold Spring Harbor Press, New York, 2003).

The terms “unique sequence tag”, “sequence tag”, “tag” or “barcode”, as used interchangeably herein, refer to an oligonucleotide that is attached to a polynucleotide or template molecule and is used to identify and/or track the polynucleotide or template in a reaction or a series of reactions. A sequence tag may be attached to the 3′- or 5′-end of a polynucleotide or template, or it may be inserted into the interior of such polynucleotide or template to form a linear conjugate, sometimes referred to herein as a “tagged polynucleotide,” or “tagged template,” or the like. Sequence tags may vary widely in size and compositions; the following references, which are incorporated herein by reference in their entireties, provide guidance for selecting sets of sequence tags appropriate for particular embodiments: Brenner, U.S. Pat. No. 5,635,400; Brenner and Macevicz, U.S. Pat. No. 7,537,897; Brenner et al, Proc. Natl. Acad. Sci., 97: 1665-1670 (2000); Church et al, European patent publication 0 303 459; Shoemaker et al, Nature Genetics, 14: 450-456 (1996); Morris et al, European patent publication 0799897A1; Wallace, U.S. Pat. No. 5,981,179; and the like. Lengths and compositions of sequence tags can vary widely, and the selection of particular lengths and/or compositions depends on several factors including, without limitation, how tags are used to generate a readout, e.g., via a hybridization reaction or via an enzymatic reaction, such as sequencing; whether they are labeled, e.g., with a fluorescent dye or the like; the number of distinguishable oligonucleotide tags required to unambiguously identify a set of polynucleotides, and the like, and how different the tags of a particular set must be in order to ensure reliable identification, e.g., freedom from cross hybridization or misidentification from sequencing errors. In one aspect, sequence tags can each have a length within a range of from about 2 to about 36 nucleotides, or from about 4 to about 30 nucleotides, or from about 4 to about 20 nucleotides, or from about 8 to about 20 nucleotides, or from about 6 to about 10 nucleotides. In one aspect, sets of sequence tags are used, wherein each sequence tag of a set has a unique nucleotide sequence that differs from that of every other tag of the same set by at least two bases; in another aspect, sets of sequence tags are used wherein the sequence of each tag of a set differs from that of every other tag of the same set by at least three bases. In some embodiments, the unique sequence tag can be a “unique molecular identifier”, or “UMI,” and can be used, for example, to differentiate various unique nucleic acid sequence fragments originating from the test sample. In other embodiments, a “sequence tag” can be used to differentiate nucleic acid sequence fragments that originate from different test samples (e.g., a sample-specific sequence tag).

The term “enrich” as used herein means to increase a proportion of one or more target nucleic acids, or one or more nucleic acids from a targeted region of a genome, in a sample. An “enriched” sample or sequencing library is therefore a sample or sequencing library in which a proportion of one of more target nucleic acids, or one or more nucleic acids from a targeted region, has been increased with respect to non-target nucleic acids, or regions, in the sample.

The terms “subject” and “patient” are used interchangeably herein and refer to a human or non-human animal who is known to have, or potentially has, a medical condition or disorder, such as, e.g., a cancer.

The term “sequence read” as used herein refers to a nucleotide sequence, obtained from or read from a nucleic acid obtained from a subject. Sequence reads can be obtained through various methods known in the art. Generally, sequence reads are obtained post-amplification (e.g., polymerase chain reaction, such as bridge amplification) of a nucleic acid fragment that is obtained or enriched from a test sample.

The term “cell free nucleic acid,” “cell free DNA,” or “cfDNA,” “cell-free RNA,” or “cfRNA,” refers to nucleic acid fragments that circulate in an individual's body (e.g., in a body fluid such as the bloodstream) and originate from one or more healthy cells and/or from one or more diseased cells (e.g., cancer cells).

The terms “circulating tumor DNA” or “ctDNA” and “circulating tumor RNA” or “ctRNA” refer to nucleic acid fragments (DNA or RNA) that originate from tumor cells or other types of cancer cells, which may be released into a subject's bloodstream as a result of biological processes, such as apoptosis or necrosis of dying cells, or may be actively released by viable tumor cells.

DETAILED DESCRIPTION OF THE INVENTION

The present invention describes various methods for preparing an enriched sequencing library from a test sample. In some embodiment, the enriched sequencing library can be used for detecting cancer, determining cancer status, monitoring cancer progression, and/or determining a cancer classification.

FIG. 1 is a flow diagram illustrating a method 100 for preparing an enriched sequencing library from a cell-free DNA test sample. As shown in FIG. 1, at step 110, a biological test sample is obtained from a subject (e.g., a patient). In one embodiment, the biological sample may be a sample selected from the group consisting of blood, plasma, serum, urine and saliva samples. In other embodiments, the sample is a plasma sample from a cancer patient, or a patient suspected of having cancer. Alternatively, the biological sample may comprise a sample selected from the group consisting of whole blood, a blood fraction, a tissue biopsy, pleural fluid, pericardial fluid, cerebral spinal fluid, and peritoneal fluid. In accordance with some embodiments, the biological test sample comprises a plurality of cell-free nucleic acids (e.g., cell-free DNA (cfDNA) or cell-free RNA (cfRNA)) fragments. In other embodiments, the biological test sample comprises a plurality of cell-free nucleic acids (e.g., cell-free DNA and RNA) fragments originating from healthy cells and from cancer cells. Optionally, in one embodiment, cell-free nucleic acids (e.g., cfDNA or cfRNA) can be extracted and/or purified from the biological test sample before proceeding with subsequent library preparation steps. In general, any known method in the art can be used to extract and purify cell-free nucleic acids from the biological test sample. For example, cell-free nucleic acids can be extracted and purified using one or more known commercially available protocols or kits, such as the QIAAMP® circulating nucleic acid kit (Qiagen).

At step 120 the cell-free nucleic acid sample (e.g., cfDNA) is used to prepare a sequencing library. In general, any known method for preparing a sequencing library can be used. For example, a standard sequencing library preparation protocol (e.g., TRUSEQ® library preparation protocol (Illumina, Inc.)) that includes the steps of end repair, 3′-end A-tailing, ligation of sequencing adapters (e.g., Y-adapters), and PCR amplification can be used to complete preparation of the sequencing library from the cfDNA test sample.

In one embodiment, the sequencing adapters can include a unique molecular identifier (UMI) sequence, such that, after library preparation, the sequencing library will include UMI tagged amplicons derived from cell-free nucleic acid fragments. In one embodiment, unique sequence tags (e.g., unique molecular identifiers (UMIs)) can be used to identify unique nucleic acid sequences from a cell-free nucleic acid sample. For example, differing unique sequence tags (UMIs) can be used to differentiate various unique nucleic acid sequence fragments originating from the test sample. In another embodiment, unique sequence tags (UMIs) can be used to reduce amplification bias, which is the asymmetric amplification of different targets due to differences in nucleic acid composition (e.g., high GC content). The unique sequence tags (UMIs) can also be used to discriminate between nucleic acid mutations that arise during amplification. The unique sequence tags can be present in a multi-functional nucleic acid sequencing adapter, which sequencing adapter can comprise both a unique sequence tag and a universal priming site. In one embodiment, the unique sequence tag can comprise a short oligonucleotide sequence having a length of from about 2 nt to about 100 nt, from about 2 nt to about 60 nt, from about 2 to about 40 nt, or from about 2 to about 20 nt. In another embodiment, the UMI tag may comprise a short oligonucleotide sequence greater than about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or 18 nucleotides (nt) in length.

In another embodiment, the sequencing adapters utilized in the practice of this invention may include a universal primer and/or one or more sequencing oligonucleotides for use in subsequent cluster generation and/or sequencing (e.g., known P5 and P7 sequences for used in sequencing by synthesis (SBS) (Illumina, San Diego, Calif.)).

At step 130 the method further comprises enriching the sequencing library using a plurality of capture probes. In accordance with some embodiments of the present invention, the plurality of capture probes comprise a set of probes selected for use in a sequencing assay to enrich for targeted nucleic acid sequences, or for nucleic acids from a targeted region of a genome. For example, nucleic acid sequences can be targeted for enrichment that are known to be, or suspected of being, informative for detecting the presence or absence of cancer, determining cancer stage, monitoring cancer progression, and/or for determining a cancer classification (e.g., cancer type and/or cancer tissue of origin). In one embodiment, as described elsewhere herein, the sequencing library is enriched for AT-rich sequences. The term “AT-rich” or “AT-rich sequence” as used herein refers to a nucleic acid sequence having greater than 50% AT content. In other embodiments, an AT-rich sequence can comprise a nucleic acid sequence having greater than 55%, 60%, 65%, 70%, 75%, or 80% AT content, or more. In another embodiment, the capture probes are selected to enrich for one or more somatic mutations indicative of cancer. In yet another embodiment, the capture probes are selected to enrich for one or more single nucleotide variants (SNVs), indels, fusion events and/or copy number alterations (CNAs) that are known to be, or may be, indicative of the presence or absence of cancer, cancer stage, and/or a cancer classification (e.g., cancer type or tissue of origin).

In accordance with some embodiments of the present invention, the plurality of capture probes can be hybridized to a complementary nucleic acid sequence within one or more specific regions (i.e., targeted sequence fragments) of the human genome and used to enrich, or isolate, nucleic acid sequences derived from the targeted region. One or more probes can be hybridized to one or more nucleic acid fragments derived from a target region to capture the one or more nucleic acid fragments and enrich for the one or more targeted nucleic acids. In one embodiment, the targeted nucleic acids-probe hybridized construct can be isolated using one or more means known in the art (as described further elsewhere herein).

In one embodiment, the plurality of capture probes can be short nucleic acids or oligonucleotides. Short nucleic acids typically have a length of 1000 nucleotide or less. In one embodiment, the capture probes used in the practice of the enrichment strategy can range in length from about 20 nt to about 200 nt, from about 30 to about 160 nt, or from about 40 to about 120 bp. In another embodiment, the probes are designed to be at least about 20 nt in length, at least about 40 nt in length, at least about 60 nt in length, or at least about 80 nt in length. In still other embodiments, the probes can be less than 80 nt length, less than 60 nt in length, less than 40 nt in length, or less than 30 nt in length. In some embodiments, the probes can be designed to overlap a specific target region. For example, the probes used in the practice of the present invention can be designed to overlap within a given target region of a targeted nucleic acid sequence. For example, in some embodiments, the probes can overlap within a target region by about 2 nt to about 60 nt, from about 10 nt to about 50 nt, from about 10 nt to about 40 nt, or from about 10 nt to about 20 nt. In one embodiment, the probes are designed to overlap within a target region of a targeted nucleic acid sequence by at least about 2 nt, at least about 5 nt, at least about 10 nt, at least about 15 nt, or at least about 20 nt.

In one embodiment, the plurality of capture probes comprises a set of capture probes designed to capture, or isolate, one or more targeted nucleic acid sequences derived from one or more target regions of the human genome. For example, in one embodiment, the probe set can target from about 5 to about 10,000, from about 10 to about 5,000, from about 20 to about 1000, of from about 30 to about 500 specific regions, or target regions within the human genome. In other embodiments, the probe set can target at least about 20, at least about 50, at least about 100 or more target regions of the human genome. In still another embodiment, the probe set can target at least about 100, at least about 500, or at least about 1,000 specific regions of the human genome. In some embodiments, the targeted nucleic acid sequences may comprise one or more genes known to be, or suspected of being indicative of cancer. In other embodiments, the targeted nucleic acids may comprise one or more single nucleotide variants (SNVs), indels, fusion events and/or copy number alterations (CNAs) that are known to be, or may be, indicative of the presence or absence of cancer, cancer status, and/or a cancer classification (e.g., cancer type or tissue of origin).

After hybridization to the one or more target regions or target nucleic acid sequences, at step 140, the hybridized capture probes can be extended to generate extended capture probes. Extending the capture probes results in an improved or increased probe-template binding efficiency, thereby reducing off-target or non-target binding, and improving the overall efficiency of the targeted isolation. For example, after hybridization to single-stranded target nucleic acids, the free 3′-ends of the probes can be extended through a polymerization reaction, utilizing the single-stranded nucleic acid fragment as a template, thereby producing an extended probe sequence. In one embodiment, the probe can be extended using a DNA or RNA polymerase. In general, any known DNA or RNA polymerase can be utilized in the step. In one embodiment, the single-stranded nucleic acid is DNA, and a DNA polymerase with strand displacement activity is used to extend the capture probes. For example, the DNA polymerase may be Bacillus stearothermophilus DNA polymerase (Bst Pol) (available from Clontech), T4 DNA polymerase (available from New England BioLabs, Inc.), or phi29 DNA polymerase (available from New England BioLabs, Inc.). Although not wishing to be bound by theory, it is believed that the use of a strand-displacement polymerase will displace random, non-target or off-target probe hybridization events. Reducing off-target, or non-target binding events allows for more diverse on-target libraries and allows for the use of more stringent washing steps, thereby improved selectivity in the enrichment process. The ability to reduce off-target, or non-target binding events also allows for the use of shorter probes which typically are less expensive and easier to design.

Finally, at step 150, the extended capture probes are used to isolate, and enrich for, targeted nucleic acid fragments from the sequencing library. In general, any known method in the art can be used to isolate probe-hybridized target nucleic acids. For example, as is well known in the art, a biotin moiety can be added to the 5′-end of the probes (i.e., biotinylated) to facilitate isolation of target nucleic acids hybridized to probes using a streptavidin-coated surface (e.g., streptavidin-coated beads).

FIG. 2 is an illustration showing pictorially the steps of a method 200 for enriching a sequencing library for one or more target nucleic acid sequences (i.e., a target region) 210, as described above with reference to FIG. 1.

As shown in FIG. 2, a set of capture probes 220 are provided, wherein the probe set 220 comprising a plurality of probes sharing sequence complementary to the target region 210. As shown in FIG. 2, the capture probe set 220 can include probes directed to both the sense 220 a and antisense 220 b strands (i.e., single-stranded DNA (ssDNA) fragments 230) derived from a plurality of double-strand DNA (dsDNA) fragments. Furthermore, as shown the sense 220 a and antisense 220 b strands can be used to target, and thereby capture, a plurality of single-stranded DNA fragments 230 that overlap the target region 210.

As shown at step 240, the sense 220 a and antisense capture probes 220 b can be hybridized to individual single-strand DNA (ssDNA) fragments contained within a test sample. The sense strand capture probes will hybridize with the sense ssDNA fragments (+ strands) and the antisense strand capture probes will hybridize with the antisense ssDNA fragments (− strands), respectively.

As shown at step 250, the hybridized probes can be extended to create extended capture probes 255. As described elsewhere herein, the hybridized probes can be extended using a polymerase (e.g., a DNA polymerase). In one embodiment, the DNA polymerase has strand-displacement activity. As described above, the use of extended capture probes 255 results in an improved or increased probe-template binding efficiency, thereby reducing off-target or non-target binding, and improving the overall efficiency of the targeted isolation.

Finally, as shown at step 260, the hybridized extended capture probe-target ssDNA fragment constructs can be washed to purify the enriched sequencing library and/or to eliminate any non-hybridized probes from the sample. As described elsewhere herein, the use of extended capture probes 255 can allow for more stringent washing steps resulting in an improved selectivity in the enrichment process.

After washing, the sequence library can be sequenced to obtain sequence data or sequence reads and the sequence data or reads analyzed. In one embodiment, the sequence data or reads can be analyzed for use in detecting cancer, determining cancer stage, monitoring cancer progression and/or classifying cancer (not shown). For example, as described elsewhere herein, the probe set can be designed to isolate, or enrich for, nucleic acid fragments that are known to be, or may be, indicative of the presence or absence of cancer, cancer stage, cancer progression, and/or a cancer classification (e.g., cancer type and/or tissue of origin).

FIG. 3 is a flow diagram illustrating a method 300 for preparing an enriched sequencing library from a cell-free DNA test sample for use in detecting cancer, determining cancer status, monitoring cancer progression, and/or determining a cancer classification.

As shown in FIG. 3, at step 310, a biological test sample is obtained from a subject (e.g., a patient) known to have or suspected of having cancer. In one embodiment, the biological sample may be a sample selected from the group consisting of blood, plasma, serum, urine and saliva samples. In other embodiments, the sample is a plasma sample from a cancer patient, or a patient suspected of having cancer. Alternatively, as noted above, the biological sample may comprise a sample selected from the group consisting of whole blood, a blood fraction, a tissue biopsy, pleural fluid, pericardial fluid, cerebral spinal fluid, and peritoneal fluid. In accordance with some embodiments, the biological test sample comprises a plurality of cell-free nucleic acids (e.g., cell-free DNA (cfDNA) or cell-free RNA (cfRNA)) fragments. In other embodiments, the biological test sample comprises a plurality of cell-free nucleic acids (e.g., cell-free DNA and RNA) fragments originating from healthy cells and from cancer cells. Optionally, in one embodiment, cell-free nucleic acids (e.g., cfDNA or cfRNA) can be extracted and/or purified from the biological test sample before proceeding with subsequent library preparation steps. In general, any known method in the art can be used to extract and purify cell-free nucleic acids from the biological test sample. For example, cell-free nucleic acids can be extracted and purified using one or more known commercially available protocols or kits, such as the QUIAAMP® circulating nucleic acid kit (Qiagen).

At step 320 the cell-free nucleic acid sample (e.g., cfDNA) is used to prepare a sequencing library. In general, any known method for preparing a sequencing library can be used. For example, a standard sequencing library preparation protocol (e.g., TRUSEQ® library preparation protocol (Illumina, Inc.)) that includes the steps of end repair, 3′-end A-tailing, ligation of sequencing adapters (e.g., Y-adapters), and PCR amplification can be used to complete preparation of the sequencing library from the cfDNA test sample.

In one embodiment, the sequencing adapters can include a unique molecular identifier (UMI) sequence, such that, after library preparation, the sequencing library will include UMI tagged amplicons derived from cell-free nucleic acid fragments. In one embodiment, as described in further detail elsewhere herein, unique sequence tags (e.g., unique molecular identifiers (UMIs)) can be used to identify unique nucleic acid sequences from a cell-free nucleic acid sample. For example, differing unique sequence tags (UMIs) can be used to differentiate various unique nucleic acid sequence fragments originating from the test sample. In another embodiment, unique sequence tags (UMIs) can be used to reduce amplification bias, which is the asymmetric amplification of different targets due to differences in nucleic acid composition (e.g., high GC content). The unique sequence tags (UMIs) can also be used to discriminate between nucleic acid mutations that arise during amplification. The unique sequence tags can be present in a multi-functional nucleic acid adapter, which adapter can comprise both a unique sequence tag and a universal priming site.

In another embodiment, the sequencing adapters utilized in the practice of the invention may include a universal primer and/or one or more sequencing oligonucleotides for use in subsequent cluster generation and/or sequencing (e.g., known P5 and P7 sequences for used in sequencing-by-synthesis (SBS) (Illumina, San Diego, Calif.)).

At step 330 the method further comprises enriching the sequencing library using a plurality of capture probes. In accordance with the present invention, the plurality of capture probes comprise a set of probes selected for use in a sequencing assay to enrich for nucleic acids sequences known to be, or that may be, indicative for cancer. For example, nucleic acid sequences can be targeted for enrichment that are known to be, or suspected of being, informative for detecting the presence or absence of cancer, determining cancer stage, monitoring cancer progression, and/or for determining a cancer classification (e.g., cancer type or cancer tissue of origin). In one embodiment, the capture probes are selected to enrich for one or more somatic mutations indicative of cancer. In another embodiment, the capture probes are selected to enrich for one or more single nucleotide variants (SNVs), indels, fusion events and/or copy number alterations (CNAs) that are known to be, or may be, indicative of the presence or absence of cancer, cancer stage, and/or a cancer classification (e.g., cancer type or tissue of origin).

In one embodiment, the plurality of capture probes can be hybridized to a complementary nucleic acid sequence within one or more specific regions (i.e., targeted sequence fragments) of the human genome and used to enrich, or isolate, nucleic acid sequences derived from the targeted region. One or more probes can be hybridized to one or more nucleic acid fragments derived from a target region to capture the one or more nucleic acid fragments and enrich for the one or more targeted nucleic acids. In one embodiment, as described elsewhere herein, the targeted nucleic acids-probe hybridized construct can be isolated using one or more means known in the art (as described further elsewhere herein).

After hybridization to the one or more target regions or target nucleic acid sequences, at step 340, the capture probes can be extended to generate extended capture probes and used to isolate, and enrich for, targeted nucleic acid fragments from the sequencing library. Extending the capture probes results in an improved or increased probe-template binding efficiency, thereby reducing off-target or non-target binding, and improving the overall efficiency of the targeted isolation. For example, after hybridization to single-stranded target nucleic acids, the free 3′-ends of the probes can be extended through a polymerization reaction, utilizing the single-stranded nucleic acid fragment as a template, thereby producing an extended probe sequence. In one embodiment, the probe can be extended using a DNA or RNA polymerase. In general, any known DNA or RNA polymerase can be utilized in the step. In one embodiment, the single-stranded nucleic acid is DNA, and a DNA polymerase with strand displacement activity is used to extend the capture probes. For example, the DNA polymerase may be Bacillus stearothermophilus DNA polymerase (Bst Pol) (available from Clontech), T4 DNA polymerase (available from New England BioLabs, Inc.), or phi29 DNA polymerase (available from New England BioLabs, Inc.). Although not wishing to be bound by theory, it is believed that the use of a strand-displacement polymerase will displace random, non-target or off-target probe hybridization events. Reducing off-target, or non-target binding events allows for more diverse on-target libraries and allows for the use of more stringent washing steps, thereby improved selectivity in the enrichment process. The ability to reduce off-target, or non-target binding events also allows for the use of shorter probes which are typically less expensive and easier to design.

Furthermore, at step 340, the extended capture probes can be used to isolate, and enrich for, targeted nucleic acid fragments from the sequencing library. In general, any known method in the art can be used to isolate probe-hybridized target nucleic acids. For example, as is well known in the art, a biotin moiety can be added to the 5′-end of the probes (i.e., biotinylated) to facilitate isolation of target nucleic acids hybridized to probes using a streptavidin-coated surface (e.g., streptavidin-coated beads).

At step 350 at least a portion of enriched sequence library is sequenced to obtain sequencing data or sequence reads, and the sequencing data or sequence reads analyzed. In general, any method known in the art can be used to obtain sequence data or sequence reads from a test sample. For example, in one embodiment, sequencing data or sequence reads from the cell-free DNA sample can be acquired using next generation sequencing (NGS). Next-generation sequencing methods include, for example, sequencing by synthesis technology (Illumina), pyrosequencing (454), ion semiconductor technology (Ion Torrent sequencing), single-molecule real-time sequencing (Pacific Biosciences), sequencing by ligation (SOLiD sequencing), and nanopore sequencing (Oxford Nanopore Technologies). In some embodiments, sequencing is massively parallel sequencing using sequencing-by-synthesis with reversible dye terminators. In other embodiments, sequencing is sequencing-by-ligation. In yet other embodiments, sequencing is single molecule sequencing. In still another embodiment, sequencing is paired-end sequencing. Optionally, an amplification step is performed prior to sequencing.

At step 360, the sequencing data or sequence reads can be analyzed for detecting the presence or absence of cancer, determining cancer stage, monitoring cancer progression, and/or for determining a cancer classification (e.g., cancer type or cancer tissue of origin). In another embodiment, the sequencing data or sequence reads can be used to infer the presence or absence of cancer, cancer status and/or a cancer classification. For example, the sequencing data or sequencing reads can be analyzed to identify one or more mutational signatures indicative of cancer (see, e.g., PCT Application No. PCT/US 2017/060472, filed Nov. 7, 2017). Alternatively, the sequencing data or sequencing reads can be modeled for the detection and/or classification of cancer (see, e.g., U.S. Patent Application No. 62/363,047, filed Feb. 27, 2018, or U.S. Patent Application No. 62/642,301, filed Mar. 13, 2018).

In one embodiment, the sequencing data or sequence reads can be analyzed to detect the presence or absence of, determine the stage of, monitor progression of, and/or classify a carcinoma, a sarcoma, a myeloma, a leukemia, a lymphoma, a blastoma, a germ cell tumor, or any combination thereof. In some embodiments, the carcinoma may be an adenocarcinoma. In other embodiments, the carcinoma may be a squamous cell carcinoma. In still other embodiments, the carcinoma is selected from the group consisting of: small cell lung cancer, non-small-cell lung, nasopharyngeal, colorectal, anal, liver, urinary bladder, cervical, testicular, ovarian, gastric, esophageal, head-and-neck, pancreatic, prostate, renal, thyroid, melanoma, and breast carcinoma. In another embodiment, the sequencing data or sequence reads can be analyzed to detect presence or absence of, determine the stage of, monitor progression of, and/or classify a sarcoma. In certain embodiments, the sarcoma can be selected from the group consisting of: osteosarcoma, chondrosarcoma, leiomyosarcoma, rhabdomyosarcoma, mesothelial sarcoma (mesothelioma), fibrosarcoma, angiosarcoma, liposarcoma, glioma, and astrocytoma. In still another embodiment, the sequencing data or sequence reads can be analyzed to detect presence or absence of, determine the stage of, monitor progression of, and/or classify leukemia. In certain embodiments, the leukemia can be selected from the group consisting of: myelogenous, granulocytic, lymphatic, lymphocytic, and lymphoblastic leukemia. In still another embodiment, the sequencing data or sequence reads can be used to detect presence or absence of, determine the stage of, monitor progression of, and/or classify a lymphoma. In certain embodiments, the lymphoma can be selected from the group consisting of: Hodgkin's lymphoma and Non-Hodgkin's lymphoma.

Sequencing and Bioinformatics

As reviewed above, aspects of the invention include sequencing of nucleic acid molecules to generate a plurality of sequence reads, compilation of a plurality of sequence reads into a sequencing library, and bioinformatic manipulation of the sequence reads and/or sequencing library to determine sequence information from a test sample (e.g., a biological sample). In some embodiments, one or more aspects of the subject methods are conducted using a suitably-programmed computer system, as described further herein.

In certain embodiments, a sample is collected from a subject, followed by enrichment for genetic regions or genetic fragments of interest. For example, in some embodiments, a sample can be enriched by hybridization to a nucleotide array comprising cancer-related genes or gene fragments of interest. In some embodiments, a sample can be enriched for genes of interest (e.g., cancer-associated genes) using other methods known in the art, such as hybrid capture. See, e.g., Lapidus (U.S. Pat. No. 7,666,593), the contents of which is incorporated by reference herein in its entirety. In one hybrid capture method, a solution-based hybridization method is used that includes the use of biotinylated oligonucleotides and streptavidin coated magnetic beads. See, e.g., Duncavage et al., J Mol Diagn. 13(3): 325-333 (2011); and Newman et al., Nat Med. 20(5): 548-554 (2014). Isolation of nucleic acid from a sample in accordance with the methods of the invention can be done according to any method known in the art.

Sequencing may be by any method or combination of methods known in the art. For example, known DNA sequencing techniques include, but are not limited to, classic dideoxy sequencing reactions (Sanger method) using labeled terminators or primers and gel separation in slab or capillary, sequencing by synthesis using reversibly terminated labeled nucleotides, pyrosequencing, 454 sequencing, allele specific hybridization to a library of labeled oligonucleotide probes, sequencing by synthesis using allele specific hybridization to a library of labeled clones that is followed by ligation, real time monitoring of the incorporation of labeled nucleotides during a polymerization step, Polony sequencing, and SOLiD sequencing. Sequencing of separated molecules has more recently been demonstrated by sequential or single extension reactions using polymerases or ligases as well as by single or sequential differential hybridizations with libraries of probes.

One conventional method to perform sequencing is by chain termination and gel separation, as described by Sanger et al., Proc Natl. Acad. Sci. USA, 74(12): 5463 67 (1977), the contents of which are incorporated by reference herein in their entirety. Another conventional sequencing method involves chemical degradation of nucleic acid fragments. See, Maxam et al., Proc. Natl. Acad. Sci., 74: 560 564 (1977), the contents of which are incorporated by reference herein in their entirety. Methods have also been developed based upon sequencing by hybridization. See, e.g., Harris et al., (U.S. patent application number 2009/0156412), the contents of which are incorporated by reference herein in their entirety.

A sequencing technique that can be used in the methods of the provided invention includes, for example, Helicos True Single Molecule Sequencing (tSMS) (Harris T. D. et al. (2008) Science 320:106-109), the contents of which are incorporated by reference herein in their entirety. Further description of tSMS is shown, for example, in Lapidus et al. (U.S. Pat. No. 7,169,560), the contents of which are incorporated by reference herein in their entirety, Lapidus et al. (U.S. patent application publication number 2009/0191565, the contents of which are incorporated by reference herein in their entirety), Quake et al. (U.S. Pat. No. 6,818,395, the contents of which are incorporated by reference herein in their entirety), Harris (U.S. Pat. No. 7,282,337, the contents of which are incorporated by reference herein in their entirety), Quake et al. (U.S. patent application publication number 2002/0164629, the contents of which are incorporated by reference herein in their entirety), and Braslaysky, et al., PNAS (USA), 100: 3960-3964 (2003), the contents of which are incorporated by reference herein in their entirety.

Another example of a DNA sequencing technique that can be used in the methods of the provided invention is 454 sequencing (Roche) (Margulies, M et al. 2005, Nature, 437, 376-380, the contents of which are incorporated by reference herein in their entirety). Another example of a DNA sequencing technique that can be used in the methods of the provided invention is SOLiD technology (Applied Biosystems). Another example of a DNA sequencing technique that can be used in the methods of the provided invention is Ion Torrent sequencing (U.S. patent application publication numbers 2009/0026082, 2009/0127589, 2010/0035252, 2010/0137143, 2010/0188073, 2010/0197507, 2010/0282617, 2010/0300559, 2010/0300895, 2010/0301398, and 2010/0304982, the contents of each of which are incorporated by reference herein in their entirety).

In some embodiments, the sequencing technology is Illumina sequencing. Illumina sequencing is based on the amplification of DNA on a solid surface using fold-back PCR and anchored primers. Genomic DNA can be fragmented, or in the case of cfDNA, fragmentation is not needed due to the already short fragments. Adapters are ligated to the 5′- and 3′-ends of the fragments. DNA fragments that are attached to the surface of flow cell channels are extended and bridge amplified. The fragments become double stranded, and the double stranded molecules are denatured. Multiple cycles of the solid-phase amplification followed by denaturation can create several million clusters of approximately 1,000 copies of single-stranded DNA molecules of the same template in each channel of the flow cell. Primers, DNA polymerase and four fluorophore-labeled, reversibly terminating nucleotides are used to perform sequential sequencing. After nucleotide incorporation, a laser is used to excite the fluorophores, and an image is captured and the identity of the first base is recorded. The 3′ terminators and fluorophores from each incorporated base are removed and the incorporation, detection and identification steps are repeated.

Another example of a sequencing technology that can be used in the methods of the provided invention includes the single molecule, real-time (SMRT) technology of Pacific Biosciences. Yet another example of a sequencing technique that can be used in the methods of the provided invention is nanopore sequencing (Soni G V and Meller A. (2007) Clin Chem 53: 1996-2001, the contents of which are incorporated by reference herein in their entirety). Another example of a sequencing technique that can be used in the methods of the provided invention involves using a chemical-sensitive field effect transistor (chemFET) array to sequence DNA (for example, as described in US Patent Application Publication No. 20090026082, the contents of which are incorporated by reference herein in their entirety). Another example of a sequencing technique that can be used in the methods of the provided invention involves using an electron microscope (Moudrianakis E. N. and Beer M. Proc Natl Acad Sci USA. 1965 March; 53:564-71, the contents of which are incorporated by reference herein in their entirety).

If the nucleic acid from the sample is degraded or only a minimal amount of nucleic acid can be obtained from the sample, PCR can be performed on the nucleic acid in order to obtain a sufficient amount of nucleic acid for sequencing (See, e.g., Mullis et al. U.S. Pat. No. 4,683,195, the contents of which are incorporated by reference herein in its entirety).

Biological Samples

Aspects of the invention involve obtaining a test sample, e.g., a biological sample, such as a tissue and/or body fluid sample, from a subject for purposes of analyzing a plurality of nucleic acids (e.g., a plurality of RNA molecules) therein. Samples in accordance with embodiments of the invention can be collected in any clinically-acceptable manner. Any test sample suspected of containing a plurality of nucleic acids can be used in conjunction with the methods of the present invention. In some embodiments, a test sample can comprise a tissue, a body fluid, or a combination thereof. In some embodiments, a biological sample is collected from a healthy subject. In some embodiments, a biological sample is collected from a subject who is known to have a particular disease or disorder (e.g., a particular cancer or tumor). In some embodiments, a biological sample is collected from a subject who is suspected of having a particular disease or disorder.

As used herein, the term “tissue” refers to a mass of connected cells and/or extracellular matrix material(s). Non-limiting examples of tissues that are commonly used in conjunction with the present methods include skin, hair, finger nails, endometrial tissue, nasal passage tissue, central nervous system (CNS) tissue, neural tissue, eye tissue, liver tissue, kidney tissue, placental tissue, mammary gland tissue, gastrointestinal tissue, musculoskeletal tissue, genitourinary tissue, bone marrow, and the like, derived from, for example, a human or non-human mammal. Tissue samples in accordance with embodiments of the invention can be prepared and provided in the form of any tissue sample types known in the art, such as, for example and without limitation, formalin-fixed paraffin-embedded (FFPE), fresh, and fresh frozen (FF) tissue samples.

As used herein, the term “body fluid” refers to a liquid material derived from a subject, e.g., a human or non-human mammal. Non-limiting examples of body fluids that are commonly used in conjunction with the present methods include mucous, blood, plasma, serum, serum derivatives, synovial fluid, lymphatic fluid, bile, phlegm, saliva, sweat, tears, sputum, amniotic fluid, menstrual fluid, vaginal fluid, semen, urine, cerebrospinal fluid (CSF), such as lumbar or ventricular CSF, gastric fluid, a liquid sample comprising one or more material(s) derived from a nasal, throat, or buccal swab, a liquid sample comprising one or more materials derived from a lavage procedure, such as a peritoneal, gastric, thoracic, or ductal lavage procedure, and the like.

In some embodiments, a test sample can comprise a fine needle aspirate or biopsied tissue. In some embodiments, a test sample can comprise media containing cells or biological material. In some embodiments, a test sample can comprise a blood clot, for example, a blood clot that has been obtained from whole blood after the serum has been removed. In some embodiments, a test sample can comprise stool. In one preferred embodiment, a test sample is drawn whole blood. In one aspect, only a portion of a whole blood sample is used, such as plasma, red blood cells, white blood cells, and platelets. In some embodiments, a test sample is separated into two or more component parts in conjunction with the present methods. For example, in some embodiments, a whole blood sample is separated into plasma, red blood cell, white blood cell, and platelet components.

In some embodiments, a test sample includes a plurality of nucleic acids not only from the subject from which the test sample was taken, but also from one or more other organisms, such as viral DNA/RNA that is present within the subject at the time of sampling.

Nucleic acid can be extracted from a test sample according to any suitable methods known in the art, and the extracted nucleic acid can be utilized in conjunction with the methods described herein. See, e.g., Maniatis, et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor, N.Y., pp. 280-281, 1982, the contents of which are incorporated by reference herein in their entirety.

In one preferred embodiment, cell free nucleic acid (e.g., cell-free DNA (cfDNA) and/or cell-free RNA (cfRNA)) are extracted from a test sample. cfDNA are short base nuclear-derived DNA fragments present in several bodily fluids (e.g. plasma, stool, urine). See, e.g., Mouliere and Rosenfeld, PNAS 112(11): 3178-3179 (Mar 2015); Jiang et al., PNAS (Mar 2015); and Mouliere et al., Mol Oncol, 8(5):927-41 (2014). Tumor-derived circulating tumor nucleic acids (e.g., ctDNA and/or ctRNA) constitutes a minority population of cfNAs (i.e., cfDNA and/or cfRNA), in some cases, varying up to about 50%. In some embodiments, ctDNA and/or ctRNA varies depending on tumor stage and tumor type. In some embodiments, ctDNA and/or ctRNA varies from about 0.001% up to about 30%, such as about 0.01% up to about 20%, such as about 0.01% up to about 10%. The covariates of ctDNA and/or ctRNA are not fully understood, but appear to be positively correlated with tumor type, tumor size, and tumor stage. E.g., Bettegowda et al, Sci Trans Med, 2014; Newmann et al, Nat Med, 2014. Despite the challenges associated with the low population of ctDNA/ctRNA in cfNAs, tumor variants have been identified in ctDNA and/or ctRNA across a wide span of cancers. E.g., Bettegowda et al, Sci Trans Med, 2014. Furthermore, analysis of cfDNA and/or cfRNA versus tumor biopsy is less invasive, and methods for analyzing, such as sequencing, enable the identification of sub-clonal heterogeneity. Analysis of cfDNA and/or cfRNA has also been shown to provide for more uniform genome-wide sequencing coverage as compared to tumor tissue biopsies. In some embodiments, a plurality of cfDNA and/or cfRNA are extracted from a sample in a manner that reduces or eliminates co-mingling of cfDNA and genomic DNA. For example, in some embodiments, a sample is processed to isolate a plurality of the cfDNA and/or cfRNA therein in less than about 2 hours, such as less than about 1.5, 1 or 0.5 hours.

A non-limiting example of a procedure for preparing nucleic acid from a blood sample follows. Blood may be collected in 10 mL EDTA tubes (for example, the BD VACUTAINER® family of products from Becton Dickinson, Franklin Lakes, N.J.), or in collection tubes that are adapted for isolation of cfDNA (for example, the CELL FREE DNA BCT® family of products from Streck, Inc., Omaha, Nebr.) can be used to minimize contamination through chemical fixation of nucleated cells, but little contamination from genomic DNA is observed when samples are processed within 2 hours or less, as is the case in some embodiments of the present methods. Beginning with a blood sample, plasma may be extracted by centrifugation, e.g., at 3000 rpm for 10 minutes at room temperature minus brake. Plasma may then be transferred to 1.5 ml tubes in 1 ml aliquots and centrifuged again at 7000 rpm for 10 minutes at room temperature. Supernatants can then be transferred to new 1.5 ml tubes. At this stage, samples can be stored at −80° C. In certain embodiments, samples can be stored at the plasma stage for later processing, as plasma may be more stable than storing extracted cfDNA and/or cfRNA.

Plasma DNA and/or RNA can be extracted using any suitable technique. For example, in some embodiments, plasma DNA and/or RNA can be extracted using one or more commercially available assays, for example, the QIAmp Circulating Nucleic Acid Kit family of products (Qiagen N.V., Venlo Netherlands). In certain embodiments, the following modified elution strategy may be used. DNA and/or RNA may be extracted using, e.g., a QIAmp Circulating Nucleic Acid Kit, following the manufacturer's instructions (maximum amount of plasma allowed per column is 5 mL). If cfDNA and/or cfRNA are being extracted from plasma where the blood was collected in Streck tubes, the reaction time with proteinase K may be doubled from 30 min to 60 min. Preferably, as large a volume as possible should be used (i.e., 5 mL). In various embodiments, a two-step elution may be used to maximize cfDNA and/or cfRNA yield. First, DNA and/or RNA can be eluted using 30 μL of buffer AVE for each column. A minimal amount of buffer necessary to completely cover the membrane can be used in the elution in order to increase cfDNA and/or cfRNA concentration. By decreasing dilution with a small amount of buffer, downstream desiccation of samples can be avoided to prevent melting of double stranded DNA or material loss. Subsequently, about 30 μL of buffer for each column can be eluted. In some embodiments, a second elution may be used to increase DNA and/or RNA yield.

In other embodiments, RNA can be extracted and/or isolated using any suitable technique. For example, in some embodiments, RNA can be extracted using a commercially-available kit and/or protocol, e.g., a QIAamp Circulating Nucleic Acids kit and micro RNA extraction protocol.

In some embodiments, the methods involve DNase treating an extracted nucleic acid sample to remove cell-free DNA from a mixed cfDNA and cfRNA test sample.

Computer Systems and Devices

Aspects of the invention described herein can be performed using any type of computing device, such as a computer, that includes a processor, e.g., a central processing unit, or any combination of computing devices where each device performs at least part of the process or method. In some embodiments, systems and methods described herein may be performed with a handheld device, e.g., a smart tablet, or a smart phone, or a specialty device produced for the system.

Methods of the invention can be performed using software, hardware, firmware, hardwiring, or combinations of any of these. Features implementing functions can also be physically located at various positions, including being distributed such that portions of functions are implemented at different physical locations (e.g., imaging apparatus in one room and host workstation in another, or in separate buildings, for example, with wireless or wired connections).

Processors suitable for the execution of computer programs include, by way of example, both general and special purpose microprocessors, and any one or more processors of any kind of digital computer. Generally, a processor will receive instructions and data from a read-only memory or a random access memory, or both. The essential elements of a computer are a processor for executing instructions and one or more memory devices for storing instructions and data. Generally, a computer will also include, or be operatively coupled to receive data from or transfer data to, or both, one or more mass storage devices for storing data, e.g., magnetic, magneto-optical disks, or optical disks. Information carriers suitable for embodying computer program instructions and data include all forms of non-volatile memory, including, by way of example, semiconductor memory devices, (e.g., EPROM, EEPROM, solid state drive (SSD), and flash memory devices); magnetic disks, (e.g., internal hard disks or removable disks); magneto-optical disks; and optical disks (e.g., CD and DVD disks). The processor and the memory can be supplemented by, or incorporated in, special purpose logic circuitry.

To provide for interaction with a user, the subject matter described herein can be implemented on a computer having an I/O device, e.g., a CRT, LCD, LED, or projection device for displaying information to the user and an input or output device such as a keyboard and a pointing device, (e.g., a mouse or a trackball), by which the user can provide input to the computer. Other kinds of devices can be used to provide for interaction with a user as well. For example, feedback provided to the user can be any form of sensory feedback, (e.g., visual feedback, auditory feedback, or tactile feedback), and input from the user can be received in any form, including acoustic, speech, or tactile input.

The subject matter described herein can be implemented in a computing system that includes a back-end component (e.g., a data server), a middleware component (e.g., an application server), or a front-end component (e.g., a client computer having a graphical user interface or a web browser through which a user can interact with an implementation of the subject matter described herein), or any combination of such back-end, middleware, and front-end components. The components of the system can be interconnected through a network by any form or medium of digital data communication, e.g., a communication network. For example, a reference set of data may be stored at a remote location and a computer can communicate across a network to access the reference data set for comparison purposes. In other embodiments, however, a reference data set can be stored locally within the computer, and the computer accesses the reference data set within the CPU for comparison purposes. Examples of communication networks include, but are not limited to, cell networks (e.g., 3G or 4G), a local area network (LAN), and a wide area network (WAN), e.g., the Internet.

The subject matter described herein can be implemented as one or more computer program products, such as one or more computer programs tangibly embodied in an information carrier (e.g., in a non-transitory computer-readable medium) for execution by, or to control the operation of, a data processing apparatus (e.g., a programmable processor, a computer, or multiple computers). A computer program (also known as a program, software, software application, app, macro, or code) can be written in any form of programming language, including compiled or interpreted languages (e.g., C, C++, Perl), and it can be deployed in any form, including as a stand-alone program or as a module, component, subroutine, or other unit suitable for use in a computing environment. Systems and methods of the invention can include instructions written in any suitable programming language known in the art, including, without limitation, C, C++, Perl, Java, ActiveX, HTML5, Visual Basic, or JavaScript.

A computer program does not necessarily correspond to a file. A program can be stored in a file or a portion of a file that holds other programs or data, in a single file dedicated to the program in question, or in multiple coordinated files (e.g., files that store one or more modules, sub-programs, or portions of code). A computer program can be deployed to be executed on one computer or on multiple computers at one site or distributed across multiple sites and interconnected by a communication network.

A file can be a digital file, for example, stored on a hard drive, SSD, CD, or other tangible, non-transitory medium. A file can be sent from one device to another over a network (e.g., as packets being sent from a server to a client, for example, through a Network Interface Card, modem, wireless card, or similar).

Writing a file according to the invention involves transforming a tangible, non-transitory computer-readable medium, for example, by adding, removing, or rearranging particles (e.g., with a net charge or dipole moment into patterns of magnetization by read/write heads), the patterns then representing new collocations of information about objective physical phenomena desired by, and useful to, the user. In some embodiments, writing involves a physical transformation of material in tangible, non-transitory computer readable media (e.g., with certain optical properties so that optical read/write devices can then read the new and useful collocation of information, e.g., burning a CD-ROM). In some embodiments, writing a file includes transforming a physical flash memory apparatus such as NAND flash memory device and storing information by transforming physical elements in an array of memory cells made from floating-gate transistors. Methods of writing a file are well-known in the art and, for example, can be invoked manually or automatically by a program or by a save command from software or a write command from a programming language.

Suitable computing devices typically include mass memory, at least one graphical user interface, at least one display device, and typically include communication between devices. The mass memory illustrates a type of computer-readable media, namely computer storage media. Computer storage media may include volatile, nonvolatile, removable, and non-removable media implemented in any method or technology for storage of information, such as computer readable instructions, data structures, program modules, or other data. Examples of computer storage media include RAM, ROM, EEPROM, flash memory, or other memory technology, CD-ROM, digital versatile disks (DVD) or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices, Radiofrequency Identification (RFID) tags or chips, or any other medium that can be used to store the desired information, and which can be accessed by a computing device.

Functions described herein can be implemented using software, hardware, firmware, hardwiring, or combinations of any of these. Any of the software can be physically located at various positions, including being distributed such that portions of the functions are implemented at different physical locations.

As one skilled in the art would recognize as necessary or best-suited for performance of the methods of the invention, a computer system for implementing some or all of the described inventive methods can include one or more processors (e.g., a central processing unit (CPU) a graphics processing unit (GPU), or both), main memory and static memory, which communicate with each other via a bus.

A processor will generally include a chip, such as a single core or multi-core chip, to provide a central processing unit (CPU). A process may be provided by a chip from Intel or AMD.

Memory can include one or more machine-readable devices on which is stored one or more sets of instructions (e.g., software) which, when executed by the processor(s) of any one of the disclosed computers can accomplish some or all of the methodologies or functions described herein. The software may also reside, completely or at least partially, within the main memory and/or within the processor during execution thereof by the computer system. Preferably, each computer includes a non-transitory memory such as a solid state drive, flash drive, disk drive, hard drive, etc.

While the machine-readable devices can in an exemplary embodiment be a single medium, the term “machine-readable device” should be taken to include a single medium or multiple media (e.g., a centralized or distributed database, and/or associated caches and servers) that store the one or more sets of instructions and/or data. These terms shall also be taken to include any medium or media that are capable of storing, encoding, or holding a set of instructions for execution by the machine and that cause the machine to perform any one or more of the methodologies of the present invention. These terms shall accordingly be taken to include, but not be limited to, one or more solid-state memories (e.g., subscriber identity module (SIM) card, secure digital card (SD card), micro SD card, or solid-state drive (SSD)), optical and magnetic media, and/or any other tangible storage medium or media.

A computer of the invention will generally include one or more I/O device such as, for example, one or more of a video display unit (e.g., a liquid crystal display (LCD) or a cathode ray tube (CRT)), an alphanumeric input device (e.g., a keyboard), a cursor control device (e.g., a mouse), a disk drive unit, a signal generation device (e.g., a speaker), a touchscreen, an accelerometer, a microphone, a cellular radio frequency antenna, and a network interface device, which can be, for example, a network interface card (NIC), Wi-Fi card, or cellular modem.

Any of the software can be physically located at various positions, including being distributed such that portions of the functions are implemented at different physical locations.

Additionally, systems of the invention can be provided to include reference data. Any suitable genomic data may be stored for use within the system. Examples include, but are not limited to: comprehensive, multi-dimensional maps of the key genomic changes in major types and subtypes of cancer from The Cancer Genome Atlas (TCGA); a catalog of genomic abnormalities from The International Cancer Genome Consortium (ICGC); a catalog of somatic mutations in cancer from COSMIC; the latest builds of the human genome and other popular model organisms; up-to-date reference SNPs from dbSNP; gold standard indels from the 1000 Genomes Project and the Broad Institute; exome capture kit annotations from Illumina, Agilent, Nimblegen, and Ion Torrent; transcript annotations; small test data for experimenting with pipelines (e.g., for new users).

In some embodiments, data is made available within the context of a database included in a system. Any suitable database structure may be used including relational databases, object-oriented databases, and others. In some embodiments, reference data is stored in a relational database such as a “not-only SQL” (NoSQL) database. In certain embodiments, a graph database is included within systems of the invention. It is also to be understood that the term “database” as used herein is not limited to one single database; rather, multiple databases can be included in a system. For example, a database can include two, three, four, five, six, seven, eight, nine, ten, fifteen, twenty, or more individual databases, including any integer of databases therein, in accordance with embodiments of the invention. For example, one database can contain public reference data, a second database can contain test data from a patient, a third database can contain data from healthy individuals, and a fourth database can contain data from sick individuals with a known condition or disorder. It is to be understood that any other configuration of databases with respect to the data contained therein is also contemplated by the methods described herein.

References and citations to other documents, such as patents, patent applications, patent publications, journals, books, papers, web contents, have been made throughout this disclosure. All such documents are hereby incorporated herein by reference in their entirety for all purposes.

Various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including references to the scientific and patent literature cited herein. The subject matter herein contains important information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof. All references cited throughout the specification are expressly incorporated by reference herein.

The foregoing detailed description of embodiments refers to the accompanying drawings, which illustrate specific embodiments of the present disclosure. Other embodiments having different structures and operations do not depart from the scope of the present disclosure. The term “the invention” or the like is used with reference to certain specific examples of the many alternative aspects or embodiments of the applicants' invention set forth in this specification, and neither its use nor its absence is intended to limit the scope of the applicants' invention or the scope of the claims. This specification is divided into sections for the convenience of the reader only. Headings should not be construed as limiting of the scope of the invention. The definitions are intended as a part of the description of the invention. It will be understood that various details of the present invention may be changed without departing from the scope of the present invention. Furthermore, the foregoing description is for the purpose of illustration only, and not for the purpose of limitation.

While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adapt to a particular situation, material, composition of matter, process, process step or steps, to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto.

EXAMPLE

To evaluate recovery of targeted nucleic acids using probe extension, an isolation comparison between non-probe extended (labeled herein as “SOP”) and probe extended (labeled herein as “PEX”) protocols was carried out.

First, 30 ng sheared NA12878 genomic DNA (gDNA) (available from Coriell Institute, Camden, N.J.) was used to prepare a sequencing library. The double-stranded DNA fragments were prepared for ligation to forked adapters by end repairing DNA ends to make them blunt-ended, phosphorylating the 5′-ends, and adding a single A nucleotide tail to the 3′-ends. Forked adapters were ligated to the repaired and A-tailed DNA fragments using T4 DNA ligase (30 min at 37° C.). Finally, the ligated reaction product is subject to multiple cycles of PCR to amplify ligated products containing adapter sequence at both ends of the double-stranded DNA fragments. After amplification, the reaction mixture was split into two aliquots and used to enrich for, and isolate, a plurality of targeted nucleic acids with and without probe extension, respectively, in accordance with the present invention.

Isolation of targeted nucleic acid sequences with probe extension (labeled herein as “PEX”). A first 2 μg aliquot was enriched for targeted nucleic acid sequences utilizing a capture probe set designed to capture, and isolate DNA fragments originating from 65 targeted regions of the human genome known to be, or suspected of being, indicative of cancer. Each of the probes in the probe set was biotinylated for subsequent isolation using streptavidin-coated beads. First, 4 ng of the probe set was added to the aliquot and incubated overnight to allow for probe-target nucleic acid hybridization. After hybridization, the probe-target nucleic acids were extracted from the reaction mixture using streptavidin-coated magnetic beads. After extraction, the streptavidin-coated magnetic beads were resuspended, and washed, using 100 μL resuspension buffer (RSB). After washing, T4 DNA polymerase reaction buffer and T4 DNA Pol (Exonuclease minus) (both available from Lucigen, Madison, Wis.) were added to the reaction mixture and probe extension was allowed to proceed for 30 min at 37° C. After probe extension, the streptavidin beads were washed to remove non-specific binding of off-target library. After washing the targeted libraries were eluted from the targeted probes using an alkali solution, the solution was neutralized and PCR amplified.

Isolation of targeted nucleic acid sequences without probe extension (labeled herein as “SOP”). The second 2 μg aliquot was also enriched for targeted nucleic acids sequences utilizing the same capture probe set designed to capture, and isolate DNA fragments originating from 65 targeted regions of the human genome known to be, or suspected of being, indicative of cancer. Each of the probes in the probe set was biotinylated for subsequent isolation using streptavidin-coated beads. 4 ng of the probe set was added to the aliquot and incubated overnight to allow for probe-target nucleic acid hybridization. After hybridization, the probe-target nucleic acids were extracted from the reaction mixture using streptavidin-coated magnetic beads. The streptavidin beads were washed to remove non-specific binding of off-target library. After washing, the targeted libraries were eluted from the targeted probes using an alkali solution, the solution was neutralized, then PCR amplified.

Finally, both of the extracted and washed reaction samples were sequenced and analyzed using an Illumina MiSeq system (Illumina, San Diego, Calif.). Both raw coverage and collapsed coverage were determined for each of the 65 nucleic acid target regions.

FIGS. 4A and 4B are bar graphs illustrating mean, and raw base coverage, respectively, for PEX and SOP samples. As shown in FIGS. 4A and 4B, both mean base coverage and raw base coverage are similar for the PEX and SOP samples.

FIG. 5 is a bar graph illustrating drop out for AT-rich DNA fragments (AT) and GC-rich (GC) DNA fragments. As shown in FIG. 5, AT-rich DNA fragment dropout was significantly reduced in the PEX sample compared to the SOP sample.

FIG. 6 is a bar graph illustrating normalized coverage for raw and collapsed sequence reads from PEX and SOP samples. As shown in FIG. 6, normalized collapsed coverages are similar for the PEX and SOP samples. However, the PEX sample shows an increase in normalized raw coverage compared to the SOP sample.

FIG. 7 is a dot plot illustrating the ratio of raw normalized coverage for each enriched target region plotted against the % GC content of the targets. An increase in raw normalized coverage was observed in PEX samples at lower % GC content (i.e., in AT-rich DNA fragments), demonstrating enrichment of AT-rich DNA fragments, relative to GC-rich DNA fragments using probe extension (PEX).

FIGS. 8A and 8B are plots for two separate sequencing runs, respectively, illustrating collapsed coverage across targeted nucleic acids for targeted regions 1, 10, 20, 30, 40 and 50. As shown in FIGS. 8A and 8B, relative coverage is increased at the 3′-end for most probe extended targets (PEX) compared to the SOP samples.

The foregoing detailed description of embodiments refers to the accompanying drawings, which illustrate specific embodiments of the present disclosure. Other embodiments having different structures and operations do not depart from the scope of the present disclosure. The term “the invention” or the like is used with reference to certain specific examples of the many alternative aspects or embodiments of the applicants' invention set forth in this specification, and neither its use nor its absence is intended to limit the scope of the applicants' invention or the scope of the claims. This specification is divided into sections for the convenience of the reader only. Headings should not be construed as limiting of the scope of the invention. The definitions are intended as a part of the description of the invention. It will be understood that various details of the present invention may be changed without departing from the scope of the present invention. Furthermore, the foregoing description is for the purpose of illustration only, and not for the purpose of limitation. 

1. A method for preparing an enriched sequencing library, the method comprising: (a) obtaining a test sample comprising a plurality of cell-free nucleic acid (cfNA) fragments; (b) preparing a sequencing library from the cfNA fragments; (c) enriching the sequencing library by: i. adding a plurality of capture probes to the sequencing library, wherein the plurality of capture probes are designed to be complementary to one or more regions of one or more target nucleic acids; ii. hybridizing the plurality of capture probes to the one or more target nucleic acids; iii. extending the capture probes using a polymerase and the target nucleic acids as a template to generate a plurality of extended probe-target nucleic acid constructs; and iv. isolating the plurality of extended probe-target nucleic acid constructs to generate the enriched sequencing library. 2.-34. (canceled)
 35. The method of claim 1, wherein the enriched sequencing library is enriched for AT-rich sequences.
 36. The method of claim 1, wherein the cfNA fragments comprise cell-free DNA (cfDNA), cell-free RNA (cfRNA), or any combination thereof.
 37. The method claim 1, wherein the plurality of capture probes range in length from about 20 nt to about 200 nt.
 38. The method of claim 1, wherein the capture probes comprise a set of probes designed to hybridize with nucleic acid fragments from about 5 to about 10,000 target regions.
 39. The method of claim 1, wherein the capture probes comprise a set of capture probes designed to hybridize with one or more sense strands and one or more antisense strands of a plurality of target nucleic acids.
 40. The method of claim 1, wherein the polymerase is a DNA polymerase having strand-displacement activity.
 41. The method of claim 1, wherein the capture probes are biotinylated capture probes.
 42. The method of claim 41, wherein the extended probe-target nucleic acids are isolated using one or more streptavidin-coated beads.
 43. The method of claim 1, wherein the test sample comprises: whole blood, a blood fraction, plasma, serum, urine, fecal matter, saliva, a tissue biopsy, pleural fluid, pericardial fluid, cerebrospinal fluid, peritoneal fluid, or any combination thereof.
 44. The method of claim 43, wherein the test sample comprises nucleic acids originating from one or more healthy cells and from one or more cancer cells.
 45. The method of claim 1, wherein the capture probes are selected to enrich for one or more single nucleotide variants (SNVs), indels, fusion events and/or copy number alterations (CNAs).
 46. A method for detecting a presence or absence of a cancer, determining a cancer stage, monitoring a cancer progression, determining a cancer classification, or any combination thereof, in a subject, the method comprising: (a) obtaining a test sample comprising a plurality of cell-free nucleic acid (cfNA) fragments; (b) preparing a sequencing library from the cfNA fragments; (c) enriching the sequencing library by: i. adding a plurality of capture probes to the sequencing library, wherein the plurality of capture probes are designed to be complementary to one or more regions of one or more target nucleic acids; ii. hybridizing the plurality of capture probes to the one or more target nucleic acids; iii. extending the capture probes using a polymerase and the target nucleic acids as a template to generate a plurality of extended probe-target nucleic acid constructs; and iv. isolating the plurality of extended probe-target nucleic acid constructs to generate the enriched sequencing library, (d) sequencing the enriched sequencing library to obtain a plurality of sequence reads; and (e) analyzing the one or more target nucleic acids in the plurality of sequence reads to detect a presence or absence of a cancer, determine a cancer status, monitor a cancer progression and/or determine a cancer classification for the test sample.
 47. The method of claim 46, wherein the test sample is a plasma sample obtained from a patient known to have, or suspected of having a cancer.
 48. The method of claim 46, wherein the sequence reads are obtained from a next-generation sequencing (NGS) procedure.
 49. The method of claim 46, wherein monitoring cancer progression further comprises monitoring disease progression, monitoring therapy, or monitoring cancer growth.
 50. The method of claim 46, wherein the cancer classification comprises determining a cancer type and/or a cancer tissue of origin.
 51. The method of claim 46, wherein the cancer comprises a carcinoma, a sarcoma, a myeloma, a leukemia, a lymphoma, a blastoma, a germ cell tumor, or any combination thereof.
 52. The method of claim 51, wherein the carcinoma is an adenocarcinoma.
 53. The method of claim 51, wherein the carcinoma is a squamous cell carcinoma.
 54. The method of claim 51, wherein the carcinoma is selected from the group consisting of: small cell lung, non-small-cell lung, nasopharyngeal, colorectal, anal, liver, urinary bladder, cervical, testicular, ovarian, gastric, esophageal, head-and-neck, pancreatic, prostate, renal, thyroid, melanoma, and breast carcinoma.
 55. The method of claim 51, wherein the sarcoma is selected from the group consisting of: osteosarcoma, chondrosarcoma, leiomyosarcoma, rhabdomyosarcoma, mesothelial sarcoma (mesothelioma), fibrosarcoma, angiosarcoma, liposarcoma, glioma, and astrocytoma.
 56. The method of claim 51, wherein the leukemia is selected from the group consisting of: myelogenous, granulocytic, lymphatic, lymphocytic, and lymphoblastic leukemia.
 57. The method of claim 51, wherein the lymphoma is selected from the group consisting of: Hodgkin's lymphoma and Non-Hodgkin's lymphoma. 